Interested in pursuing Postgraduate GMP qualifications in 2027? Applications to join our next cohort in March 2027 close soon?
Paper logbooks are still everywhere on GMP manufacturing floors. They do the job, but they cost more than most sites realise.
Training has always been important in regulated industries, especially for those involved in the manufacture and handling of pharmaceuticals, medical devices and healthcare products.
In the medical device industry, internal audits are often viewed primarily as a regulatory requirement. ISO 13485:2016 requires organisations to assess the effectiveness of their Quality Management System (QMS). However, organisations that treat internal auditing purely as a compliance exercise risk missing a significant opportunity.
Good Manufacturing Practice (GMP) Needs to Move Beyond Training Records
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Ready to lead in the world of pharmaceutical manufacturing?
The future of quality management is no longer about forcing processes into rigid systems; it is about empowering organisations to design quality around their unique needs. That’s exactly where MasterControl’s Advanced Quality Event Management (AQEM) comes in.
SAP ECC6 has been an Enterprise Resource Planning (ERP) workhorse for decades, but its lifecycle is coming to an end. SAP has already ended support for older ECC versions (EHP 0–5) as of 31 December 2025 and SAP has announced that mainstream support for ECC (EHP6-8) will end in 2027; with extended maintenance options to 2030 for an additional fee.
SeerPharma and the University of Technology Sydney (UTS) have been strategic partners for over 10 years, delivering postgraduate qualifications in Good Manufacturing Practice (GMP). This program provides a pathway to an industry-recognised qualification, whether you are launching your career or preparing to step into a more senior role in Quality...
Paper manufacturing records usually fail in the same predictable ways: missed fields, illegible handwriting, manual calculations, messy corrections, missing signatures, and not enough context when something goes wrong. The results are also predictable: more deviations, slower batch release, and uncomfortable audit discussions because the evidence...
